Home / Recalls / Medical Devices
Hamilton Medical AG recalls IntelliCuff, Portable automatic cuff pressure controller REF: 951001
Recalled July 8, 2026 · FDA recall Z-2625-2026 · Hamilton Medical AG
Hazard
Due to reported complaints, the cuff device may alarm with a "Cuff System Leakage" error. As a result, the motor may pump continuously and fail to maintain the cuff pressure set by the user. · FDA Class II
Units
962 units
Sold at
Worldwide - US Nationwide distribution in the states of AZ, CA, CO, FL, GA, HI, IL, KY, MA, MI, ND, NE, NE, NY, OH, PA, PR, SD, TX, VA, WA, WI, WV, WY and the country of Canada.
Description
Due to reported complaints, the cuff device may alarm with a "Cuff System Leakage" error. As a result, the motor may pump continuously and fail to maintain the cuff pressure set by the user.
Product
IntelliCuff, Portable automatic cuff pressure controller REF: 951001
Manufacturer(s)
Hamilton Medical AG
Made in
Switzerland
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →